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FDA 510(k)

QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM

K-Number: K895147 · 1990-02-23

ApplicantQuantum Intl.
Decision Date1990-02-23
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Quantum Intl.. It received FDA 510(k) clearance on 1990-02-23 under 510(k) number K895147. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM?

QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1990-02-23. The listed applicant is Quantum Intl.. The 510(k) number is K895147.

When did QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM receive FDA 510(k) clearance?

QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM received FDA 510(k) clearance on 1990-02-23, under 510(k) number K895147.

Who is the listed applicant for QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM?

The FDA 510(k) record lists Quantum Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM?

The FDA product code for QUANTUM QAD-1E ANGIODYNOGRAPH ULTRASOUND SYSTEM is IYO.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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